is a genetic disorder causing early, severe iron overload and organ damage.

is an inherited kidney disorder causing scarring, cysts, and progressive dysfunction.

is a rare muscle disease causing progressive hip and shoulder weakness.

is a rare benign blood vessel growth that appears on the skin.

is a cancer of the lymphatic system that often responds to treatment.

is a cancer of the lymphatic system with specific abnormal cells.

is the most common Hodgkin lymphoma subtype, often affecting young adults.

is a rare, usually slow-growing type of Hodgkin lymphoma.

is an eye condition involving a small hole or fluid-filled cyst.

is a rare nerve condition causing a sluggish pupil and reduced reflexes.

is a rare inherited biotin-processing disorder causing metabolic crises, often treatable.

is a brain malformation where the forebrain fails to separate properly.

is a rare genetic brain development disorder affecting the brain and face.

is a genetic holoprosencephaly subtype variably affecting early brain and facial development.

is a rare genetic condition where the forebrain does not divide normally.

is a genetic disorder affecting early brain and facial development.

is a rare genetic condition affecting early brain and facial development.

is a rare genetic condition affecting early brain and facial development.

is a rare genetic condition affecting early brain and facial development.

is a rare genetic disorder affecting early brain and facial development.

is a rare genetic condition that disrupts normal brain development.

is a genetic condition where the forebrain fails to fully divide.

is a rare birth condition affecting brain, face, spine, and lower body.

is a rare genetic condition affecting early brain and skull development.